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Spiro-Polymerization: Polytocopherols as Antioxidants

Spiro-Polymerization: Polytocopherols as Antioxidants

Thomas Rosenau (ORCID: 0000-0002-6636-9260)
  • Grant DOI 10.55776/P19081
  • Funding program Principal Investigator Projects
  • Status ended
  • Start November 1, 2006
  • End December 31, 2010
  • Funding amount € 126,472

Disciplines

Chemistry (85%); Physics, Astronomy (15%)

Keywords

    Spiro-Polymerization, Polyradicals, Tocopherols, Vitamin E, Electron Paramagnetic Resonance, Antioxidants, Synthesis

Abstract Final report

Phenolic antioxidants, such as tocopherols (vitamin E), have manifold physiological functions as lipophilic radical scavengers, being used in a huge variety of medications, healthcare products, food additives, cosmetics, and polymer stabilizers. The present 3-year project deals with the development of novel phenolic "super-antioxidants" which contain many phenol (tocopherol) units per molecule, so that a hitherto unmatched antioxidative localization and efficiency can be achieved. These compounds will be synthesized according to a novel reaction sequence (spiro-polymerization / reduction); the products - long linear or cyclic alkanes with dozens or hundreds of regularly distributed phenol or vitamin E units attached ("polytocopherols") - are a completely new compound class, which opens ample ground for basic research. Synthesis, chemistry, structure-property relationships and applications of these novel and versatile compound class will be investigated within the present project. The theoretical foundation of spiro-polymerization and the regioselectivity of spiro/pyrano-pairing will be studied by computations, which will moreover be correlated to experimental data. The super-antioxidative compounds will be comprehensively analytically characterized by a combination of methods involving liquid and solid-state nuclear magnetic resonance spectroscopy, mass spectrometry and multi- detector size exclusion chromatography. They will be tested, both in vitro and in biological model systems, in terms of their antioxidative efficiency and radical-scavenging capacity, as they are promising candidates, for instance, as physiologically compatible stabilizers for polymers in food packing, or as medicinal preparations for protection of cellular membranes against the attack of reactive oxygen species, especially against oxidative burst events with high radical output due to their high concentration of antioxidatively active phenolic groups. The super-antioxidants are furthermore starting materials for the preparation of polyradicals, which are not only theoretically interesting, but also as organic magnets in materials science or as high-power spin labels, i.e. tags for molecules to better follow biochemical processes. The polyradicals properties will be studied by radical-related spectroscopic techniques (EPR, ENDOR) and correlated with theoretical work. The project work will be carried out within the framework of national and international cooperations, in collaboration with groups in Vienna, Oxford, Haifa, and Berlin.

Phenolic antioxidants, such as tocopherols (vitamin E), have manifold physiological functions as lipophilic radical scavengers, being used in a huge variety of medications, healthcare products, food additives, cosmetics, and polymer stabilizers. The present 3-year project deals with the development of novel phenolic "super-antioxidants" which contain many phenol (tocopherol) units per molecule, so that a hitherto unmatched antioxidative localization and efficiency can be achieved. These compounds will be synthesized according to a novel reaction sequence (spiro-polymerization / reduction); the products - long linear or cyclic alkanes with dozens or hundreds of regularly distributed phenol or vitamin E units attached ("polytocopherols") - are a completely new compound class, which opens ample ground for basic research. Synthesis, chemistry, structure-property relationships and applications of these novel and versatile compound class will be investigated within the present project. The theoretical foundation of spiro-polymerization and the regioselectivity of spiro/pyrano-pairing will be studied by computations, which will moreover be correlated to experimental data. The super-antioxidative compounds will be comprehensively analytically characterized by a combination of methods involving liquid and solid-state nuclear magnetic resonance spectroscopy, mass spectrometry and multi- detector size exclusion chromatography. They will be tested, both in vitro and in biological model systems, in terms of their antioxidative efficiency and radical-scavenging capacity, as they are promising candidates, for instance, as physiologically compatible stabilizers for polymers in food packing, or as medicinal preparations for protection of cellular membranes against the attack of reactive oxygen species, especially against oxidative burst events with high radical output due to their high concentration of antioxidatively active phenolic groups. The super- antioxidants are furthermore starting materials for the preparation of polyradicals, which are not only theoretically interesting, but also as organic magnets in materials science or as high-power spin labels, i.e. tags for molecules to better follow biochemical processes. The polyradicals` properties will be studied by radical-related spectroscopic techniques (EPR, ENDOR) and correlated with theoretical work. The project work will be carried out within the framework of national and international cooperations, in collaboration with groups in Vienna, Oxford, Haifa, and Berlin.

Research institution(s)
  • Universität für Bodenkultur Wien - 100%
International project participants
  • Christian Jäger, Bundesanstalt für Materialforschung und -prüfung - Germany
  • Amnon Stanger, Technion - Israel Institute of Technology - Israel
  • Christiane Timmel, University of Oxford

Research Output

  • 32 Citations
  • 4 Publications
Publications
  • 2008
    Title A Novel Dimer of a-Tocopherol
    DOI 10.1155/2008/742590
    Type Journal Article
    Author Patel A
    Journal Organic Chemistry International
    Pages 1-4
    Link Publication
  • 2009
    Title Ortho-Quinone Methides in Tocopherol Chemistry
    DOI 10.1002/9780470452882.ch6
    Type Book Chapter
    Author Rosenau T
    Publisher Wiley
    Pages 163-215
  • 2009
    Title Bromination of Non-a-Tocopherols: A Comparative Synthetic, Kinetic and Computational Study
    DOI 10.1002/ejoc.200900495
    Type Journal Article
    Author Patel A
    Journal European Journal of Organic Chemistry
    Pages 4873-4881
  • 2011
    Title On the dimers of ß-tocopherol
    DOI 10.1016/j.tet.2011.05.006
    Type Journal Article
    Author Böhmdorfer S
    Journal Tetrahedron
    Pages 4858-4861

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